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Ni-rich layered oxides are promising cathode materials for lithium-ion batteries but require improved stability to meet performance demands. To address this, doping and surface modification are commonly employed stabilization strategies, each offering distinct benefits. Doping primarily suppresses phase transitions, thereby reducing volume changes, while surface coatings protect the material by minimizing continuous reactions with electrolytes during cycling. Consequently, these approaches are often used in combination to enhance material stability. This study demonstrates that a crystalline disordered surface layer can effectively suppress structural changes without doping. Notably, the thickness of the disordered surface layer is successfully controlled during synthesis for the first time. The results reveal that the formation rate of the layered structure plays a critical role in controlling the rock-salt disordered surface layer. Although a thicker crystalline disordered surface layer in single-crystal LiNiO₂ resulted in a slight capacity reduction, it exhibits significantly improved capacity retention, maintaining up to 84% of its capacity after 500 cycles in a full-cell test, while also substantially reducing voltage decay. This study provides insights, demonstrating that well-controlled surface modification can simultaneously protect the surface and mitigate structural changes, paving the way for the development of stable cathode materials.
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http://dx.doi.org/10.1002/advs.202503476 | DOI Listing |
Adv Sci (Weinh)
September 2025
Guangxi Key Laboratory of Clean Pulp & Papermaking and Pollution Control, School of Light Industry and Food Engineering, Guangxi University, Nanning, 530004, China.
Carbonized wood has great potential as a self-supported electrode for energy storage/conversion applications. However, developing efficient and economical bifunctional electrodes by customizing the surface structure remains a challenge. This study proposes a novel multifunctional electrode design strategy, using N/P co-doped carbonized wood (NPCW) as carriers and in situ grows copper nanoparticles (Cu NPs) as nucleation centers to induce vertical growth of CuCo-layered double hydroxid (LDH) nanosheets along the substrate.
View Article and Find Full Text PDFAcc Chem Res
September 2025
Department of Pharmaceutical Chemistry and Small Molecule Discovery Center, University of California, San Francisco 94158, United States.
ConspectusProtein-protein interactions (PPIs) play a key role in homeostasis and are often dysregulated in disease. PPIs were traditionally considered "undruggable" due to their flat surfaces and disordered domains. Recently, the identification of PPI stabilizers, or molecular glues (MGs), compounds that bind cooperatively to PPI interfaces, has provided a new direction for the field.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Materials Genome Institute, Shanghai University, 200444 Shanghai, China.
High-entropy materials (HEMs) have garnered intense attention due to their unique properties derived from compositional complexity, demonstrating promise in a wide range of applications, from catalysis to energy storage and beyond. Traditionally, HEMs have been primarily concerned with metal alloys. However, expanding the principle to organic systems, specifically high-entropy molecular nanostructures, remains underexplored.
View Article and Find Full Text PDFScience
September 2025
School of Materials Engineering, Purdue University, West Lafayette, IN, USA.
In compositionally complex materials, there is controversy on the effect of enthalpy versus entropy on the structure and short-range ordering in so-called high-entropy materials. To help address this controversy, we synthesized and probed 40 MAlC layered carbide phases containing two to nine metals and found that short-range ordering from enthalpy was present until the entropy increased enough to achieve complete disordering of the transition metals in their atomic planes. We transformed all of these layered carbide phases into two-dimensional (2D) sheets and showed the effects of the order versus disorder on their surface properties and electronic behavior.
View Article and Find Full Text PDFNanoscale Adv
August 2025
Departamento de Física, Universidad de Oviedo Calvo Sotelo 18 33007 Oviedo Spain
Carbon-encapsulated γ-FeO nanoparticles (NPs) with emerging proximity effects were synthesized using a single-step solid-state pyrolysis at 750 °C. The morphology and size distribution of the NPs were investigated using high-resolution transmission and scanning electron microscopies revealing that the γ-FeO NPs, with an average diameter of 9 nm, are embedded in the amorphous porous carbon matrix. In addition, other trace phases (FeC and metallic-Fe) were also detected through X-ray absorption spectroscopy and Mössbauer spectrometry.
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